IP Library Granted Patent US 12,371,683
Granted Patent B2
US 12,371,683 · App. 16/628,258 · Granted Jul 29, 2025

Hyaluronidase variants and pharmaceutical composition comprising the same

Inventors: Soon Jae Park (Daejeon, KR); Hye-Shin Chung (Daejeon, KR); Seung Joo Lee (Daejeon, KR); Sun-Ah You (Daejeon, KR); Hyung-Nam Song (Daejeon, KR); Chang Woo Lee (Daejeon, KR)
Assignee: ALTEOGEN Inc.
C12N9/2402A61K45/06C07K14/00C12Y302/01035
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Quick Facts
Patent No.
US 12,371,683
App. No.
16/628,258
Granted
Jul 29, 2025
Kind
B2
Abstract

The present invention is related to the field of protein engineering technology which increases the enzymatic activity and thermal stability of human hyaluronidase which is an enzyme that hydrolyzes hyaluronic acid; and more particularly to hyaluronidase PH20 variants or fragments thereof, which comprise one or more amino acid residue substitutions in the region corresponding to the alpha-helix region and its linker region in the amino acid sequence of wild-type PH20 of SEQ ID NO: 1 and in which one or more amino acid residues at the N-terminus and/or the C-terminus are selectively cleaved additionally. Specifically, the present invention relates to PH20 variants or fragments thereof, which comprise one or more amino acid residue substitutions selected from the group consisting of T341A, T341C, T341G, S343E, M345T, K349E, L353A, L354I, N356E and I361T in wild-type PH20 having the amino acid sequence of SEQ ID NO: 1, and additionally comprise the substitution of amino acids located in the alpha-helix 8 region and/or a linker region between alpha-helix 7 and alpha-helix 8 in the amino acid sequence of wild-type PH20, and in which one or more amino acids located at the N-terminal and C-terminal regions are deleted.

Claims (87)

1. A PH20 variant, wherein the amino acid sequence of the PH20 variant is SEQ ID NO: 1 with modifications consisting of:

(a) amino acid residue substitutions M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D and I361T relative to SEQ ID NO: 1, and one or more amino acid residue substitutions selected from the group consisting of T341A, T341G, T341S, L342W, S343E, I344N and N363G relative to SEQ ID NO: 1;

(b) an N-terminus deletion of amino acid residues M1 to T35, M1 to L36, M1 to N37, M1 to F38, M1 to R39, or M1 to A40 of SEQ ID NO: 1; and

(c) a C-terminus deletion, wherein the C-terminus of the PH20 variant ends with an amino acid residue selected from any one of I465 to S490 of SEQ ID NO: 1.

2. The PH20 variant of claim 1 , wherein the amino acid residue substitutions relative to SEQ ID NO: 1 consist of the amino acid residue substitutions in any one of the following groups of amino acid residue substitutions:

(a) T341S, L342W, S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D and I361T;

(b) L342W, S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D and I361T;

(c) M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, I361T and N363G;

(d) T341G, L342W, S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D and I361T;

(e) T341A, L342W, S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D and I361T;

(f) I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D and 1361T; and

(g) S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D and I361T.

3. The PH20 variant of claim 1 , wherein the C-terminus of the PH20 variant ends with amino acid residue I465, D466, A467, F468, K470, P471, P472, M473, E474, T475, E476, P478, 1480, Y482, A484, P486, T488, or S490 of SEQ ID NO: 1.

4. A PH20 variant comprising the amino acid sequence of any one of the amino acid sequences of SEQ ID NOs: 60, 63 to 69, 71 to 74, 77 to 80, 82, and 87 to 115.

5. A PH20 variant comprising the amino acid sequence of SEQ ID NO: 99.

6. The PH20 variant of claim 4 , wherein the amino acid sequence of the PH20 variant consists of any one of the amino acid sequences of SEQ ID NOs: 60, 63 to 69, 71 to 74, 77 to 80, 82, and 87 to 115.

7. A PH20 variant, wherein the amino acid sequence of the PH20 variant consists of the amino acid sequence of SEQ ID NO:99.

8. A PH20 variant, wherein the amino acid sequence of the PH20 variant is SEQ ID NO: 1 with modifications consisting of:

(a) amino acid residue substitutions consisting of T341S, L342W, S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, and I361T relative to SEQ ID NO: 1;

(b) an N-terminus deletion of amino acid residues M1 to T35, M1 to L36, M1 to N37, M1 to F38, M1 to R39, or M1 to A40; and

(c) a C-terminus deletion, wherein the C-terminus of the PH20 variant ends with an amino acid residue selected from any one of I465 to S490 of SEQ ID NO: 1.

9. The PH20 variant of claim 8 , wherein the N-terminus deletion is a deletion of amino acid residues M1 to T35, M1 to L36, M1 to N37, or M1 to F38 of SEQ ID NO: 1.

10. The PH20 variant of claim 8 , wherein the N-terminus deletion is a deletion of amino acid residues M1 to T35, M1 to L36, M1 to N37, or M1 to F38 of SEQ ID NO: 1, and the C-terminus of the PH20 variant ends with amino acid residue I465, D466, A467, F468, K470, P471, P472, M473, E474, T475, E476, P478, I480, Y482, A484, P486, T488, or S490 of SEQ ID NO: 1.

11. The PH20 variant of claim 8 , wherein the N-terminus deletion is a deletion of amino acid residues M1 to T35, M1 to L36, M1 to N37, or M1 to F38 of SEQ ID NO: 1, and the C-terminus of the PH20 variant ends with amino acid residue I465, F468, or P471 of SEQ ID NO: 1.

12. The PH20 variant of claim 8 , wherein the N-terminus deletion is a deletion of amino acid residues M1 to T35, M1 to L36, M1 to N37, M1 to F38, or M1 to R39 of SEQ ID NO: 1, and the C-terminus of the PH20 variant ends with amino acid residue F468 of SEQ ID NO: 1.

13. The PH20 variant of claim 12 , wherein the N-terminus deletion is a deletion of amino acid residues M1 to T35, M1 to L36, M1 to N37, or M1 to F38 of SEQ ID NO: 1.

14. A PH20 variant, wherein the amino acid sequence of the PH20 variant is SEQ ID NO: 1 with modifications consisting of:

(a) amino acid residue substitutions, wherein the amino acid residue substitutions consist of amino acid residue substitutions in the region T341 to I361 of SEQ ID NO: 1, wherein the amino acid residue substitutions in the region T341 to 1361 comprise amino acid residue substitutions M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, and I361T relative to SEQ ID NO: 1, and one or more amino acid residue substitutions selected from the group consisting of T341A, T341C, T341D, T341G, T341S, L342W, and S343E relative to SEQ ID NO: 1, and wherein the amino acid residue substitutions in the region do not comprise an amino acid residue substitution at amino acid residue C351 or Y357 relative to SEQ ID NO: 1;

(b) an N-terminus deletion of amino acid residues M1 to T35, M1 to L36, M1 to N37, M1 to F38, M1 to R39, or M1 to A40 of SEQ ID NO: 1; and

(c) a C-terminus deletion, wherein the C-terminus of the PH20 variant ends with an amino acid residue selected from any one of I465 to S490 of SEQ ID NO: 1.

15. The PH20 variant of claim 14 , wherein the one or more amino acid residue substitutions is selected from the group consisting of T341A, T341G, T341S, L342W, and S343E relative to SEQ ID NO: 1.

16. The PH20 variant of claim 14 , wherein the amino acid residue substitutions in the region consist of the amino acid residue substitutions in any one of the following groups of amino acid residue substitutions:

(a) T341S, L342W, S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, and I361T;

(b) L342W, S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, and I361T;

(c) T341D, L342W, S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, and 1361T;

(d) T341G, L342W, S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, and I361T;

(e) T341A, L342W, S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, and I361T;

(f) T341C, L342W, S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, and I361T; and

(g) S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, and I361T.

17. The PH20 variant of claim 1 , wherein the C-terminus of the PH20 variant ends with an amino acid residue selected from any one of D466 to S490 of SEQ ID NO: 1.

18. The PH20 variant of claim 1 , wherein the one or more amino acid residue substitutions is selected from the group consisting of T341S, L342W, S343E, I344N, and N363G relative to SEQ ID NO: 1.

19. A PH20 variant comprising the amino acid sequence of SEQ ID NO: 60, 63, 64, 65, 66, 67, 68, 69, 71, 72, 73, 74, 77, 78, 79, 80, 82, 87, 88, 89, 90, 91, 92, 93, 94, 95, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 112, 113, 114, or 115.

20. The PH20 variant of claim 19 , wherein the amino acid sequence of the PH20 variant consists of the amino acid sequence of SEQ ID NO: 60, 63, 64, 65, 66, 67, 68, 69, 71, 72, 73, 74, 77, 78, 79, 80, 82, 87, 88, 89, 90, 91, 92, 93, 94, 95, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 112, 113, 114, or 115.

21. The PH20 variant of claim 1 , wherein the C-terminus of the PH20 variant ends with amino acid residue I465, D466, A467, F468, K470, P471, P472, M473, E474, T475, E476, P478, 1480, or Y482 of SEQ ID NO: 1.

22. The PH20 variant of claim 1 , wherein the N-terminus deletion is a deletion of amino acid residues M1 to T35, M1 to L36, M1 to N37, or M1 to F38 of SEQ ID NO: 1, and wherein the C-terminus of the PH20 variant ends with amino acid residue I465, D466, A467, F468, K470, P471, P472, M473, E474, T475, E476, P478, 1480, or Y482 of SEQ ID NO: 1.

23. The PH20 variant of claim 8 , wherein the N-terminus deletion is a deletion of amino acid residues M1 to T35, M1 to L36, M1 to N37, or M1 to F38 of SEQ ID NO: 1, and wherein the C-terminus of the PH20 variant ends with amino acid residue I465, D466, A467, F468, K470, P471, P472, M473, E474, T475, E476, P478, 1480, or Y482 of SEQ ID NO: 1.

24. The PH20 variant of claim 8 , wherein the N-terminus deletion is a deletion of amino acid residues M1 to T35, M1 to L36, M1 to N37, M1 to F38, or M1 to R39 of SEQ ID NO: 1.

25. The PH20 variant of claim 8 , wherein the C-terminus of the PH20 variant ends with amino acid residue F468 of SEQ ID NO: 1.

26. The PH20 variant of claim 2 , wherein the C-terminus of the PH20 variant ends with amino acid residue F468 of SEQ ID NO: 1.

27. The PH20 variant of claim 8 , wherein the C-terminus of the PH20 variant ends with amino acid residue Y482 of SEQ ID NO: 1.

28. The PH20 variant of claim 24 , wherein the C-terminus of the PH20 variant ends with amino acid residue Y482 of SEQ ID NO: 1.

29. The PH20 variant of claim 8 , wherein the C-terminus of the PH20 variant ends with amino acid residue I465, D466, A467, F468, K470, or P471 of SEQ ID NO: 1.

30. The PH20 variant of claim 24 , wherein the C-terminus of the PH20 variant ends with amino acid residue I465, D466, A467, F468, K470, or P471 of SEQ ID NO: 1.

31. A PH20 variant, wherein the amino acid sequence of the PH20 variant is SEQ ID NO: 1 with modifications consisting of:

(a) amino acid residue substitutions consisting essentially of amino acid residue substitutions in the region T341 to 1361 of SEQ ID NO: 1, wherein the amino acid residue substitutions in the region T341 to 1361 comprise amino acid residue substitutions M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, and I361T relative to SEQ ID NO: 1, and one or more amino acid residue substitutions selected from the group consisting of T341A, T341C, T341D, T341G, T341S, L342W, and S343E relative to SEQ ID NO: 1, and wherein the amino acid residue substitutions in the region do not comprise an amino acid residue substitution at amino acid residue C351 or Y357 relative to SEQ ID NO: 1;

(b) an N-terminus deletion of amino acid residues M1 to T35, M1 to L36, M1 to N37, M1 to F38, M1 to R39, or M1 to A40 of SEQ ID NO: 1; and

(c) a C-terminus deletion, wherein the C-terminus of the PH20 variant ends with an amino acid residue selected from any one of 1465 to S490 of SEQ ID NO: 1.

32. The PH20 variant of claim 31 , wherein the one or more amino acid residue substitutions is selected from the group consisting of T341A, T341G, T341S, L342W, and S343E relative to SEQ ID NO: 1.

33. The PH20 variant of claim 31 , wherein the amino acid residue substitutions in the region consist of the amino acid residue substitutions in any one of the following groups of amino acid residue substitutions:

(a) T341S, L342W, S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, and I361T;

(b) L342W, S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, and I361T;

(c) T341D, L342W, S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, and I361T;

(d) T341G, L342W, S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, and I361T;

(e) T341A, L342W, S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, and I361T;

(f) T341C, L342W, S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, and I361T; and

(g) S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, and I361T.

34. The PH20 variant of claim 31 , wherein the amino acid residue substitutions in the region consist of T341S, L342W, S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, and I361T relative to SEQ ID NO: 1.

35. The PH20 variant of claim 31 , wherein the amino acid residue substitutions in the region consist of T341S, L342W, S343E, I344N, M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D, and I361T relative to SEQ ID NO: 1, and the N-terminus deletion is a deletion of amino acid residues M1 to T35, M1 to L36, M1 to N37, or M1 to F38 of SEQ ID NO: 1.

36. A PH20 variant, wherein the amino acid sequence of the PH20 variant is SEQ ID NO: 1 with modifications consisting of:

(a) amino acid residue substitutions relative to SEQ ID NO: 1, wherein the amino acid residue substitutions consist essentially of:

amino acid residue substitutions M345T, S347T, M348K, K349E, L352Q, L353A, L354I, D355K, N356E, E359D and I361T relative to SEQ ID NO: 1, and

one or more amino acid residue substitutions selected from the group consisting of T341A, T341G, T341S, L342W, S343E, I344N and N363G relative to SEQ ID NO: 1;

(b) an N-terminus deletion of amino acid residues M1 to T35, M1 to L36, M1 to N37, M1 to F38, M1 to R39, or M1 to A40 of SEQ ID NO: 1; and

(c) a C-terminus deletion, wherein the C-terminus of the PH20 variant ends with an amino acid residue selected from any one of 1465 to S490 of SEQ ID NO: 1.

37. The PH20 variant of claim 36 , wherein the C-terminus of the PH20 variant ends with amino acid residue I465, D466, A467, F468, K470, P471, P472, M473, E474, T475, E476, P478, 1480, Y482, A484, P486, T488, or S490 of SEQ ID NO: 1.

38. The PH20 variant of claim 36 , wherein the C-terminus of the PH20 variant ends with an amino acid residue selected from any one of D466 to S490 of SEQ ID NO: 1.

39. The PH20 variant of claim 36 , wherein the one or more amino acid residue substitutions is selected from the group consisting of T341S, L342W, S343E, I344N, and N363G relative to SEQ ID NO: 1.

40. The PH20 variant of claim 36 , wherein the C-terminus of the PH20 variant ends with amino acid residue I465, D466, A467, F468, K470, P471, P472, M473, E474, T475, E476, P478, 1480, or Y482 of SEQ ID NO: 1.

41. The PH20 variant of claim 36 , wherein the N-terminus deletion is a deletion of amino acid residues M1 to T35, M1 to L36, M1 to N37, or M1 to F38 of SEQ ID NO: 1, and wherein the C-terminus of the PH20 variant ends with amino acid residue I465, D466, A467, F468, K470, P471, P472, M473, E474, T475, E476, P478, 1480, or Y482 of SEQ ID NO: 1.

42. A protein comprising the PH20 variant of claim 1 .

43. A protein comprising the PH20 variant of claim 2 .

44. A protein comprising the PH20 variant of claim 8 .

45. A protein comprising the PH20 variant of claim 14 .

46. A protein comprising the PH20 variant of claim 16 .

47. A protein comprising the PH20 variant of claim 31 .

48. A protein comprising the PH20 variant of claim 33 .

49. A protein comprising the PH20 variant of claim 36 .

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT THE THE NAME OF THE ASSIGNEE PREVIOUSLY RECORDED AT REEL: 51479 FRAME: 634. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Nov 15, 2024
From: PARK, SOON JAE; CHUNG, HYE-SHIN; LEE, SEUNG JOO; YOU, SUN-AH; SONG, HYUNG-NAM; LEE, CHANG WOO
To: ALTEOGEN INC.
Reel/Frame 070343/0657 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2020
From: PARK, SOON JAE; CHUNG, HYE-SHIN; LEE, SEUNG JOO; YOU, SUN-AH; SONG, HYUNG-NAM; LEE, CHANG WOO
To: ALTEOGEN, INC.
Reel/Frame 051479/0634 →
Priority Claims (2)
KR 10-2018-0086308 · Jul 25, 2018 · national
KR 10-2019-0029758 · Mar 15, 2019 · national
Continuity (1)
Related Publication 20210155913A1 · May 27, 2021
References Cited (379)
US 5721348A · Primakoff et al. · 1998 [cited by applicant]
US 5854046A · Au-Young et al. · 1998 [cited by applicant]
US 7767429B2 · Bookbinder · 2010 [cited by examiner]
US 8105586B2 · Bookbinder et al. · 2012 [cited by applicant]
US 8202517B2 · Bookbinder et al. · 2012 [cited by applicant]
US 8257699B2 · Bookbinder et al. · 2012 [cited by applicant]
US 8288142B2 · Uvarkina et al. · 2012 [cited by applicant]
US 8431124B2 · Bookbinder et al. · 2013 [cited by applicant]
US 8431380B2 · Bookbinder et al. · 2013 [cited by applicant]
US 8450470B2 · Bookbinder et al. · 2013 [cited by applicant]
US 8580252B2 · Bookbinder et al. · 2013 [cited by applicant]
US 8765685B2 · Bookbinder et al. · 2014 [cited by applicant]
US 8772246B2 · Bookbinder et al. · 2014 [cited by applicant]
US 8927249B2 · Wei et al. · 2015 [cited by applicant]
US 9211315B2 · Bookbinder et al. · 2015 [cited by applicant]
US 9284543B2 · Wei et al. · 2016 [cited by applicant]
US 9447401B2 · Wei et al. · 2016 [cited by applicant]
US 9562223B2 · Bookbinder et al. · 2017 [cited by applicant]
US 9677061B2 · Bookbinder et al. · 2017 [cited by applicant]
US 9677062B2 · Bookbinder et al. · 2017 [cited by applicant]
US 10286044B2 · Bookbinder et al. · 2019 [cited by applicant]
US 10328130B2 · Frost et al. · 2019 [cited by applicant]
US 10865400B2 · Wei et al. · 2020 [cited by applicant]
US 10898551B2 · Bookbinder et al. · 2021 [cited by applicant]
US 10918736B2 · Kim et al. · 2021 [cited by applicant]
US 11041149B2 · Wei et al. · 2021 [cited by applicant]
US 11066656B2 · Wei et al. · 2021 [cited by applicant]
US 11723959B2 · Bookbinder et al. · 2023 [cited by applicant]
US 11952600B2 · Wei et al. · 2024 [cited by applicant]
US 12091692B2 · Wei et al. · 2024 [cited by applicant]
US 12104185B2 · Wei et al. · 2024 [cited by applicant]
US 20060104968A1 · Bookbinder et al. · 2006 [cited by applicant]
US 20090123367A1 · Bookbinder et al. · 2009 [cited by applicant]
US 20100003238A1 · Frost et al. · 2010 [cited by applicant]
US 20100143457A1 · Wei et al. · 2010 [cited by applicant]
US 20100305500A1 · Lambert et al. · 2010 [cited by applicant]
US 20110044977A1 · Adler · 2011 [cited by applicant]
US 20120148535A1 · Carrio et al. · 2012 [cited by applicant]
US 20130101577A9 · Wei et al. · 2013 [cited by applicant]
US 20130302275A1 · Wei et al. · 2013 [cited by applicant]
US 20140037613A1 · Bookbinder et al. · 2014 [cited by applicant]
US 20140199282A1 · Bookbinder et al. · 2014 [cited by applicant]
US 20150001529A1 · Kurokawa · 2015 [cited by applicant]
US 20150010529A1 · Wei · 2015 [cited by applicant]
US 20150165059A1 · Bookbinder et al. · 2015 [cited by applicant]
US 20160362670A1 · Wei et al. · 2016 [cited by applicant]
US 20170089914A1 · Loo et al. · 2017 [cited by applicant]
US 20170218069A1 · Rosengren et al. · 2017 [cited by applicant]
US 20170218382A1 · Kondo · 2017 [cited by applicant]
US 20180044419A9 · Rosengren et al. · 2018 [cited by applicant]
US 20180185506A1 · Bookbinder et al. · 2018 [cited by applicant]
US 20180250397A1 · Benyunes et al. · 2018 [cited by applicant]
US 20190046657A1 · Kim et al. · 2019 [cited by applicant]
US 20210155913A1 · Park · 2021 [cited by applicant]
US 20210363270A1 · Park · 2021 [cited by examiner]
US 20220089738A1 · Krishnamachari et al. · 2022 [cited by applicant]
US 20220289864A1 · Park · 2022 [cited by examiner]
US 20220031093A1 · Park et al. · 2022 [cited by applicant]
US 20230174963A1 · Park et al. · 2023 [cited by applicant]
US 20230250408A1 · Park et al. · 2023 [cited by applicant]
US 20230321203A1 · Bookbinder et al. · 2023 [cited by applicant]
US 20230365692A1 · Krishnamachari et al. · 2023 [cited by applicant]
CN 101970650A · 2011 [cited by applicant]
CN 102065886A · 2011 [cited by applicant]
CN 102307993A · 2012 [cited by applicant]
CN 103173474A · 2013 [cited by applicant]
CN 104244968A · 2014 [cited by applicant]
CN 104745553A · 2015 [cited by applicant]
CN 105567606A · 2016 [cited by applicant]
CN 110494450A · 2019 [cited by applicant]
CN 111971387A · 2023 [cited by applicant]
CO 2021011944A2 · 2021 [cited by applicant]
EA 022752B1 · 2016 [cited by applicant]
EP 2405015A2 · 2012 [cited by applicant]
EP 2662090A1 · 2013 [cited by applicant]
EP 2674487A1 · 2013 [cited by applicant]
EP 1858926B1 · 2015 [cited by applicant]
EP 3037529A1 · 2016 [cited by applicant]
EP 3045472A1 · 2016 [cited by applicant]
EP 2797622B1 · 2016 [cited by applicant]
EP 3186281B1 · 2019 [cited by applicant]
EP 3130347B1 · 2019 [cited by applicant]
EP 3636752A1 · 2020 [cited by applicant]
EP 3785701A1 · 2021 [cited by applicant]
ES 2573462T3 · 2016 [cited by applicant]
JP 2009515521A · 2009 [cited by applicant]
JP 2011512844A · 2011 [cited by applicant]
JP 2015504666A · 2015 [cited by applicant]
JP 2020500863A · 2020 [cited by applicant]
JP H7166478B2 · 2022 [cited by applicant]
KR 1020120094493A · 2012 [cited by applicant]
KR 1020120105426A · 2012 [cited by applicant]
KR 101233457B1 · 2013 [cited by applicant]
KR 1020130116386A · 2013 [cited by applicant]
KR 101363658B1 · 2014 [cited by applicant]
KR 1020140021046A · 2014 [cited by applicant]
KR 101493644B1 · 2015 [cited by applicant]
KR 101546563B1 · 2015 [cited by applicant]
KR 1020160052812A · 2016 [cited by applicant]
KR 101647932B1 · 2016 [cited by applicant]
KR 1020170065032 · 2017 [cited by applicant]
KR 101874401B1 · 2018 [cited by applicant]
KR 1020200017538A · 2020 [cited by applicant]
KR 1020200130451A · 2020 [cited by applicant]
KR 1020100135291A · 2020 [cited by applicant]
KR 1020210023798A · 2021 [cited by applicant]
KR 1020220069045 · 2022 [cited by applicant]
TW 201534726A · 2015 [cited by applicant]
TW 202140780A · 2021 [cited by applicant]
WO 2004078140A2 · 2004 [cited by applicant]
WO 2007064437A2 · 2007 [cited by applicant]
WO 2009065507A2 · 2009 [cited by applicant]
WO 2009117085A1 · 2009 [cited by applicant]
WO 2009128917A2 · 2009 [cited by applicant]
WO 2010077297A1 · 2010 [cited by applicant]
WO 2011012637A2 · 2011 [cited by applicant]
WO 2011029892A2 · 2011 [cited by applicant]
WO 2012135408A1 · 2012 [cited by applicant]
WO 2013102144A2 · 2013 [cited by applicant]
WO 2015003167A1 · 2015 [cited by applicant]
WO 2015071366A1 · 2015 [cited by applicant]
WO 2015095418A1 · 2015 [cited by applicant]
WO 2016033555A1 · 2016 [cited by applicant]
WO 2017004706A1 · 2017 [cited by applicant]
WO 2017079150A1 · 2017 [cited by applicant]
WO 2017131496A1 · 2017 [cited by applicant]
WO 2018102372A1 · 2018 [cited by applicant]
WO 2018183928A1 · 2018 [cited by applicant]
WO 2018204368A1 · 2018 [cited by applicant]
WO 2018222722A2 · 2018 [cited by applicant]
WO 2019222435A1 · 2019 [cited by applicant]
WO 2020022791A1 · 2020 [cited by applicant]
WO 2020197230A1 · 2020 [cited by applicant]
WO 2020172621A1 · 2020 [cited by applicant]
WO 2021150079A1 · 2021 [cited by applicant]
WO 2022031093A1 · 2022 [cited by applicant]
WO 2023075506A1 · 2023 [cited by applicant]
PDF NCBI Reference Sequence : NP_001166492.1 (downloaded Aug. 24, 2023). (Year: 2023). [cited by examiner]
Lin et al., “Molecular cloning of the human and monkey sperm surface protein PH-20”, Proc. Natl. Aca. Sci. Vol. 90, pp. 10071-10075 (Nov. 1993). [cited by examiner]
NCBI, “NCBI Reference Sequence: XP_011728213.1haluronidase PH-20 [Macaca nemestrina]”, Apr. 24, 2018. [cited by applicant]
Arming, S., et al., “In Vitro Mutagenesis of PH-20 Hyaluronidase from Human Sperm”, “Eur. J. Biochem.”, 1997, pp. 810-814, vol. 247. [cited by applicant]
Bookbinder, L.H., et al., “A Recombinant Human Enzyme for Enhanced Interstitial Transport of Therapeutics”, “Journal of Controlled Release”, 2006, pp. 230-241, vol. 114. [cited by applicant]
Chao, K., et al., “Structure of Human Hyaluronidase-1, a Hyaluronan Hydrolyzing Enzyme Involved in Tumor Growth and Angiogenesis”, “Biochemistry”, 2007, pp. 6911-6920, vol. 46. [cited by applicant]
Frost, G. I., “Recombinant Human Hyaluronidase (rHuPH20): an Enabling Platform for Subcutaneous Drug and Fluid Administration”, “Expert Opinion Drug Delivery”, 2007, pp. 427-440, vol. 4, No. 4. [cited by applicant]
Shpilberg, O., et al., “Subcutaneous administration of rituximab MabThera and trastuzumab Herceptin using hyaluronidase”, British Journal of Cancer, 2013, pp. 1556-1561, vol. 109. [cited by applicant]
Stern, R., et al., “Mammalian Hyaluronidases”, Glycoforum, 2000, pp. 1-6, vol. 4. [cited by applicant]
Stern, R., et al., “Hyaluronidases: Their Genomics, Structures, and Mechanisms of Action”, Chem Rev, 2006, pp. 818-839, vol. 106, Publisher: American Chemical Society. [cited by applicant]
Stern, R., et al., “Supplementary Data: Hyaluronidases: Their Genomics, Structures, and Mechanisms of Action”, Chem Rev, 2006, pp. 818-839, vol. 106, Publisher: American Chemical Society. [cited by applicant]
Thomas, J.R., et al., “The INFUSE Morphine Study: Use of Recombinant Human Hyaluronidase rHuPH20 to Enhance the Absorption of Subcutaneously Administered Morphine in Patients with Advanced Illness”, Journal of Pain and … [cited by applicant]
Wang, W, et al., “Antibody Structure, Instability, and Formulation”, Journal of Pharmaceutical Sciences, DOI: 10.1002/jps.20727, 2007, vol. 96, No. 1, Publisher: Wiley InterScience. [cited by applicant]
Bittner, B., et al., “Subcutaneous Administration of Biotherapeutics An Overview of Current Challenges and Opportunities”, BioDrugs, 2018, pp. 425-440, vol. 32, Publisher: CrossMark. [cited by applicant]
Borders, C.L., et al., “Purification and Partial Characterization of Testicular Hyaluronidase”, The Journal of Biological Chemistry, 1968, pp. 3756-3762, vol. 243, No. 13. [cited by applicant]
Chen, K-J, et al., “Constitutive expression of recombinant human hyaluronidase PH20 by Pichia pastoris”, Journal of Bioscience and Bioengineering, 2016, pp. 673-678, vol. 122, Publisher: Elsevier. [cited by applicant]
Opposition filed Jan. 13, 2022 by Laboratorios Legrand S.A. against Columbian Patent Application No. NC2021/0012380, in Spanish. [cited by applicant]
English Translation of Opposition filed Jan. 13, 2022 by Laboratorios Legrand S.A. against Columbian Patent Application No. NC20210012380. [cited by applicant]
Opposition dated Jul. 5, 2022 by Asociacion de Laboratorios Farmaceuticos (ALAFAR) Against Ecuadorian Application No. SENADI-2021-70640, in Spanish. [cited by applicant]
English Translation of Opposition dated Jul. 5, 2022 by Asociacion de Laboratorios Farmaceuticos (ALAFAR) Against Ecuadorian Application No. SENADI-2021-70640. [cited by applicant]
Frost, G.I, et al., “A Microtiter-Based Assay for Hyaluronidase Activity Not Requiring Specialized Reagents”, Analytical Biochemistry, 1997, pp. 263-269, vol. 251, Publisher: Academic Press. [cited by applicant]
Hofinger, E.SA, et al., “Kinetics of Hyal 1 and PH 20 hyaluronidases: Comparison of minimal substrates and analysis of the transglycosylation reaction”, Blycobiology, 2007, pp. 963-971, vol. 17, No. 9. [cited by applicant]
Markovic Housley, Z., et al., “Crystal Structure of Hyaluronidase, a Major Allergen of Bee Venom”, Structure, 2000, pp. 1025-1035, vol. 8, Publisher: Elsevier. [cited by applicant]
Kreidieh, F.Y., et al., “Overview prevention and management of chemotherapy extravasation”, World Journal of Clinical Oncology, 2016, pp. 87-97, vol. 7, No. 1. [cited by applicant]
Mcatee, C.O., et al., “Emerging roles for hyaluronidase in cancer metastasis and therapy”, Advance in Cancer Research, 2014, pp. 1-23, vol. 123, Publisher: HHS Public Access. [cited by applicant]
Messina, L., et al., “Identification and characterization of a bacterial hyaluronidase and its production in recombinant form”, FEBS Letters, 2016, pp. 2180-2189, vol. 590, Publisher: FEB Press. [cited by applicant]
Muller, S., et al., “Spliceosomal Peptide P140 for Immunotherapy of Systemic Lupus Erythematosus”, Arthritis & Rheumatism, 2008, pp. 3873-3883, vol. 58, No. 12. [cited by applicant]
English Translation of International Search Report and Written Opinion for International Patent Application No. PCT/KR20/03975. [cited by applicant]
International Search Report Mailed Oct. 29, 2019 for PCT Application No. PCT/KR19/09215. [cited by applicant]
JP2022211105—Notice of Reasons for Refusal mailed on Nov. 14, 2023, 17 pages. [cited by applicant]
CN201980023392.4—First Office Action mailed on Jun. 17, 2023, 9 pages. [cited by applicant]
KR20207002955—Written Decision on Registration mailed on Aug. 25, 2020, 16 pages. [cited by applicant]
JP2020500863—Notice of Reasons for Refusal mailed on Jan. 25, 2022, 7 pages. [cited by applicant]
JP2020500863—Notice of Reasons for Refusal mailed on May 24, 2022, 6 pages. [cited by applicant]
JP2020500863—Notice of Reasons for Refusal mailed on Jun. 15, 2021, 12 pages. [cited by applicant]
EP19827585—Supplementary European search report mailed on Mar. 31, 2021, 9 pages. [cited by applicant]
JP2022211105—Decision of Rejection mailed on May 14, 2024, 2 pages. [cited by applicant]
CA3,093,885—Examiner Requisition mailed on Sep. 1, 2021, 4 pages. [cited by applicant]
CA3,093,885—Examiner Requisition mailed on Oct. 3, 2022, 6 pages. [cited by applicant]
AU2019311658—Examination Report No. 1 mailed on Jun. 17, 2022, 3 pages. [cited by applicant]
AU2019311658—Notice of Acceptance mailed on Oct. 11, 2022, 3 pages. [cited by applicant]
U.S. Appl. No. 17/608,729—Requirement for Restriction/Election mailed on May 14, 2024, 5 pages. [cited by applicant]
KR20227013211—Request for the Submission of an Opinion mailed on Apr. 26, 2024, 7 pages. [cited by applicant]
CN202180003323.4—First Office Action mailed on Nov. 27, 2023, 14 pages. [cited by applicant]
EP21743774—Supplementary European search report mailed on Jan. 4, 2023, 20 pages. [cited by applicant]
JP2021567961—Decision of Rejection mailed on Nov. 14, 2023, 8 pages. [cited by applicant]
JP2021567961—Notice of Reasons for Refusal mailed on Apr. 11, 2023, 6 pages. [cited by applicant]
AU2021211348—Examination Report No. 1 mailed on Mar. 17, 2023, 3 pages. [cited by applicant]
AU2021211348—Examination Report No. 2 mailed on Jul. 11, 2023, 5 pages. [cited by applicant]
AU2021211348—Notice of Acceptance mailed on Sep. 21, 2023, 4 pages. [cited by applicant]
CA3,137,324—Examiner Requisition mailed on Dec. 2, 2022, 4 pages. [cited by applicant]
CA3,137,324—Examiner Requisition mailed on May 6, 2024, 6 pages. [cited by applicant]
KR20207030248—Written Decision on Registration mailed on Dec. 22, 2023, 5 pages. [cited by applicant]
KR20207030248—Notice of Final Rejection mailed on Jul. 27, 2023, 6 pages. [cited by applicant]
KR20207030248—Request for the Submission of an Opinion mailed on Aug. 28, 2022, 14 pages. [cited by applicant]
KR20227016935—Written Decision on Registration mailed on Dec. 21, 2022, 6 pages. [cited by applicant]
JP2022068166—Notice of Reasons for Refusal mailed on Jun. 21, 2022, 8 pages. [cited by applicant]
JP2022068166—Decision to Grant a Patent mailed on Oct. 4, 2022, 5 pages. [cited by applicant]
JP2020569741—Notice of Reasons for Refusal mailed on Nov. 16, 2021, 8 pages. [cited by applicant]
JP2020569741—Decision to Grant a Patent mailed on May 16, 2023, 5 pages. [cited by applicant]
CN202310416462.0—Notification of grant of patent right for invention mailed on May 16, 2024, 3 pages. [cited by applicant]
AU2020248612—Examination Report No. 3 mailed on Nov. 8, 2023, 2 pages. [cited by applicant]
AU2020248612—Examination Report No. 2 mailed on Oct. 25, 2023, 3 pages. [cited by applicant]
CA3131052—Office Action mailed on May 6, 2024, 5 pages. [cited by applicant]
EP20776465.5—Extended European search report mailed on Feb. 11, 2022, 15 pages. [cited by applicant]
KR20210103530—Request for the Submission of an Opinion mailed on Sep. 19, 2023, 7 pages. [cited by applicant]
RU2022125351—Office Action mailed on Nov. 2, 2023, 15 pages. [cited by applicant]
International Search Report and Written Opinion dated Nov. 18, 2021 in International Application No. PCT/KR2021/010368, pp. 17. [cited by applicant]
RU2021132331—Office Action mailed on Nov. 3, 2023, 16 pages. [cited by applicant]
Appendix A Sequence Alignment, 2024, 2 pages. [cited by applicant]
AU2020248612—Notice of Acceptance mailed on Sep. 21, 2023, 4 pages. [cited by applicant]
JP2022211105—Decision of Dismissal of Amendment mailed on May 14, 2024, 4 pages. [cited by applicant]
JP2021567961—Office Action mailed on Jul. 2, 2024, 6 pages. [cited by applicant]
CN202180003323.4—First Office Action mailed on Jul. 10, 2024, 12 pages. [cited by applicant]
Tavares, A. et al., “Inhibition of the checkpoint protein PD-1 by the therapeutic antibody pembrolizumab outlined by quantum chemistry”, Scientific Reports, 2018, vol. 8, Issue 1840, pp. 1-13. [cited by applicant]
CONC20210012380—Office Action mailed on Jan. 11, 2024, 16 pages. [cited by applicant]
EA202192588—Office Action mailed on Sep. 29, 2023, 8 pages. [cited by applicant]
IDP00202108509—Office Action mailed on Sep. 27, 2023, 4 pages. [cited by applicant]
PA93644-01—Search Report mailed on Mar. 29, 2022, 8 pages. [cited by applicant]
JP2023026863—Notice of Reasons for Refusal mailed on Mar. 12, 2024, 10 pages. [cited by applicant]
CN202080003052.8—First Office Action mailed on Jun. 27, 2023, 12 pages. [cited by applicant]
CN202080003052.8—Second Office Action mailed on Mar. 2, 2024, 11 pages. [cited by applicant]
CN202310416462.0—First Office Action mailed on Mar. 5, 2024, 8 pages. [cited by applicant]
EESR Issued in counterpart European Patent Application No. 21743774.8 on Jan. 4, 2023, 20 pages. [cited by applicant]
Seffernick, J.L., et al., “Melamine Deaminase and Atrazine Chlorohydrolase: 98 Percent Identical but Functionally Different”, Journal of Bacteriology, 2001, vol. 183, No. 8, Publisher: American Society for Microbiology,… [cited by applicant]
Locke, K.W., et al., “ENHANZE drug delivery technology: a novel approach to subcutaneous administration using recombinant human hyaluronidase PH20”, Drug Delivery, 2019, DOI:10.1080/10717544.2018.1551442, vol. 26, No. 1… [cited by applicant]
Muchmore, D.B., et al., “Accelerating and Improving the Consistency of Rapid-Acting Analog Insulin Absorption and Action for Both Subcutaneous Injection and Continuous Subcutaneous Infusion Using Recombinant Human Hyalu… [cited by applicant]
Restelli, V., et al., “The Effect of Dissolved Oxygen on the Production and the Glycosylation Profile of Recombinant Human Erythropoietin Produced From CHO Cells”, Biotechnol Bioeng, 2006, vol. 9, 481-494 pages. [cited by applicant]
Schilling, S., et al., “Heterologous Expression and Characterization of Human Glutaminy Cyclase: Evidence for a Disulfide Bond with Importance for Catalytic Activity”, Biochemistry, 2002, vol. 41, Publisher: American Ch… [cited by applicant]
CA3173310—Office action mailed on Dec. 20, 2023, 5 pages. [cited by applicant]
CN202180030097.9—First Office Action mailed on Jan. 6, 2024, 19 pages. [cited by applicant]
JP2022559471—Final Notification of Reasons forRefusal mailed on Mar. 19, 2024, 8 pages. [cited by applicant]
KR1020210103530—Written Decision on Registration mailed on Dec. 15, 2023, 6 pages. [cited by applicant]
Zarrintaj et al., “Poloxamer: A versatile tri-block copolymer for biomedical applications”, Acta Biomaterialia, 2020, vol. 110, 37-67 pages. [cited by applicant]
Strickley et al., “A review of formulations of commercially available antibodies”, Journal of Pharmaceutical Sciences, 2021, vol. 110, 2590-2608 pages. [cited by applicant]
International Search Report dated Feb. 2, 2023 in International Application No. PCT/KR2022/016709, 14 pages. [cited by applicant]
CN201980023392.4—Second Office Action mailed on Feb. 8, 2024, 8 pages. [cited by applicant]
Office Action Issued in Japanese Patent Application No. 2022559471 on Oct. 11, 2023, 15 pages. [cited by applicant]
Chica et al., “Semi-rational approaches to engineering enzyme activity: combining the benefits of directed evolution and rational design” Current Opinion Biotechnology, vol. 16, Issue 4, 2005, 378-784 pages. [cited by applicant]
Wasserman, R.L., “Overview of recombinant human hyaluronidase-faciliated subcutaneous infusion of IgG in primary immunodeficiencies”, Immunotherapy, 2014, vol. 6, No. 5, Publisher: Future Medicin, 553-567 pages. [cited by applicant]
Hiromoto, Y., et al., “An Activity-Straining Method on Filtration Paper Enables High-Throughput Screening of Temperature-Sensitive and Inactive Mutations of Rice-Amylase for Improvement of Rice Grain Quality”, Plant and… [cited by applicant]
Chen, K., et al., “Constitutive Expression of Recombinant Human Hyaluronidase PH20 by Pichia Pastoris”, “Journal of Bioscience and Bioengineering”, 2016, 1-6 pages. [cited by applicant]
Office Action issued in Korean Patent Application No. 20227016935 on Aug. 28, 2022, 20 pages. [cited by applicant]
Office Action issued in Japanese Patent Application No. 2020569741 on Aug. 23, 2022, 5 pages. [cited by applicant]
Office Action issued in Canadian Patent Application No. 3131052 on Oct. 19, 2022, 6 pages. [cited by applicant]
Office Action issued in Australian Patent Application No. 2020248612 on Nov. 8, 2022, 3 pages. [cited by applicant]
Takahashi, T. et al., “A fluorimetric Morgan-Elson assay method for hyaluronidase activity,” Analytical Biochemistry, 2003, vol. 322, 257-263 pages. [cited by applicant]
John S Philo, “A Critical Review of Methods for Size Characterization of Non-Particulate Protein Aggregates,” Current Pharmaceutical Biotechnology, Jul. 2009, vol. 10, 359-372 pages. [cited by applicant]
Lafaro et al., “The Paradoxical Web of Pancreatic Cancer Tumor Microenvironment”, The American Journal of Pathology, vol. 189, No. 1, Jan. 2019, 44-57 pages. [cited by applicant]
Schon, et al., “Denatured state aggregation parameters derived from concentration dependence of protein stability”, Analytical Biochemistry, 2015, vol. 488, 45-50 pages. [cited by applicant]
NCBI Genbank Accession No. AAC60607.2, Jun. 5, 2000, 1 page. [cited by applicant]
U.S. Appl. No. 17/052,952—Non-Final Office Action mailed on Dec. 12, 2023, 32 pages. [cited by applicant]
International Search Report and Written Opinion mailed Jul. 29, 2021 for International Patent Application No. PCT/KR2021/000943 filed Mar. 24, 2020, 21 pages. [cited by applicant]
International Search Report and Written Opinion mailed Jun. 30, 2020 for International Patent Application No. PCT/KR2020/003975 filed Mar. 24, 2020, 23 pages. [cited by applicant]
The abstract of Alley et al., Journal of Thoracic Oncology, 2018, vol. 12, No. 1S, S294, Abstract No. OA13.03, 1 page. [cited by applicant]
U.S. Appl. No. 17/907,538—Requirement for Restriction/Election mailed on May 12, 2023, 5 pages. [cited by applicant]
U.S. Appl. No. 17/907,538—Non-Final Office Action mailed on Aug. 3, 2023, 10 pages. [cited by applicant]
U.S. Appl. No. 17/907,538—Ex Parte Quayle Action mailed on Feb. 15, 2024, 4 pages. [cited by applicant]
U.S. Appl. No. 17/907,538—Notice of Allowance mailed on Apr. 24, 2024, 7 pages. [cited by applicant]
CA3137324—Office Action mailed on May 6, 2024, 6 pages. [cited by applicant]
Chan et al., “Therapeutic antibodies for autoimmunity and inflammation”, Nature Reviews Immunology, vol. 10, May 2010, pp. 301-316. [cited by applicant]
Liu, “Pharmacokinetics of monoclonal antibodies and Fc-fusion proteins”, Protein Cell, 2018, vol. 9, No. 1, pp. 15-32. [cited by applicant]
NCBI Reference Sequence: NP 001166492.1 , hyaluronidase PH-20 precursor [Cavia porcelius], Jun. 21, 2021, pp. 2. [cited by applicant]
NCBI Reference Sequence: NP 001166492.1 , hyaluronidase PH-20 precursor [Cavia porcelius], Jun. 19, 2020, pp. 2. [cited by applicant]
Office Action issued in Chile Patent Application No. 202102464 with English Translation on May 4, 2023, pp. 23. [cited by applicant]
Opposition filed against Ecuador Patent Application SENADI-2021-70640 with English Translation on Feb. 14, 2022, p. 217. English Translation on Apr. 3, 2023,. [cited by applicant]
Office Action issued in Georgian Patent Application No. AP202015767 with pp. 9. [cited by applicant]
Office Action issued in Saudia Arabia Patent Application No. 521430398 with English Translation on Feb. 25, 2023, pp. 11. [cited by applicant]
Opposition by Laboratorios Legrand S.A. Against Columbian Patent Application NC20210012380 with English Translation Oct. 20, 2021, pp. 21. [cited by applicant]
Office Action issued on Dec. 2, 2022 in counterpart Canadian Patent Application No. 2137324, pp. 4. [cited by applicant]
Office Action issued on Oct. 17, 2022 in counterpart Russian Patent Application No. 2021132331, pp. 18. [cited by applicant]
Office Action issued on Sep. 5, 2022 in counterpart Taiwan Patent Application 110130965, pp. 6. [cited by applicant]
Harb, G., et al., “Safety and pharmakokinetics of subcutaneous ceftriaxone administered with or without recombinant human hyaluronidase (rHuPH20) versus intravenous ceftriaxone administration in adult volunteers”, Curre… [cited by applicant]
Broun, P., et al., “Catalytic Plasticity of Fatty Acid Modification Enzymes Underlying Chemical Diversity of Plant D Lipids”, Science, 1998, pp. 1315-1317, vol. 282, No. 13, Publisher: www.sciencemag.org. [cited by applicant]
Harris, R.J., et al., “Commercial Manufacturing Scale Formulation and Analytical Characterization of Therapeutic Recombinant Antibodies”, Drug Development Research, 2004, vol. 61, pp. 137-154. [cited by applicant]
Krantz, E.M., “Low-Dose Intramuscular Ketamine and Hyaluronidase for Induction of Anaesthesia in NonPemedicated Children”, S.A. Med. J., 1980, vol. 58, No. 4, pp. 161-162. [cited by applicant]
Whisstock, J.D., et al., “Prediction of protein function from protein sequence and structure”, Quarterly Reviews of Biophysics, 2003, vol. 36, No. 3, Publisher: Cambridge University Press, pp. 307-340. [cited by applicant]
Pakula, A., et al., “Genetic Analysis of Protein Stability and Function”, Annu. Rev. Genet., 1898, vol. 23, pp. 289-310. [cited by applicant]
Witkowski, A., et al., “Conversion of a Beta-Ketoacyl Synthase to a Malonyl Decarboxylase by Replacement of the Active-Site Cysteine with Glutamine”, Biochemistry, 1999, vol. 38, Publisher: American Chemical Society, pp… [cited by applicant]
“GenBank: AAC6067.2, PH-20 (Homo sapiens)” , NCBI , Jun. 5, 2000, pp. 2. [cited by applicant]
Singh et al., “Protein Engineering Approaches in the Post-Genomic Era”, Current Protein and Peptide Science, 2017 , vol. 18 , pp. 1-11. [cited by applicant]
Tachibana, H., et al., “Changes of monosacharide availability of human hybridoma lead to alteration of biological properties of human monoclonal antibody”, Cytotechnology, 1994, vol. 16, Publisher: Kiuwer Academic Publi… [cited by applicant]
Borys, M.C., et al., “Culture pH Affects Expression Rates and Glycosylation of Recombinant Mouse Placental Lactogen Proteins by Chinese Hamster Ovary (CHO) Cells”, Biotechnology, 1993, vol. 11, Publisher: Nature Publish… [cited by applicant]
Borys, M.C., et al., “Ammonia Affects the Glycosylation Patterns of Recombinant Mouse Placental Lactogen-| by Chinese Hamster Overy Cells in a pH-Dependent Manner”, Biotechnology and Bioengineering, 1994, vol. 43, Publi… [cited by applicant]
Clark, K.J.R., et al., “Temperature Effects on Product-Quality-Related Enzymes in Batch CHO Cell Cultures Producing Recombinant tPA”, Biotechnol. Prog., 2004, pp. 1888-1892, vol. 20, Publisher: American Chemical Society. [cited by applicant]
Clement, Wa, et al., “The use of hyaluronidase in nasal infiltration: prospective randomized controlled pilot study”, The Journal of Laryngology & Otology, 2003, vol. 117, pp. 614-618. [cited by applicant]
H. Johansen, et al., “High-level production of fully active human alpha 1-antitrypsin in [cited by applicant]
J.H. Dunham, et al., “GPR37 Surface Expression Enhancement via N-Terminal Truncation or Protein-Protein Interactions”, Biochemistry (2009) 48, pp. 10286-10297. [cited by applicant]
M. Wei, et al., “N-terminal truncations on L1 proteins of human papillomaviruses promote their soluble expression in [cited by applicant]
M. F. Meyer, et al., “The soluble hyaluronidase from bull testes is a fragment of the membrane-bound PH-20 enzyme”, FEBS letter (1997) vol. 413, pp. 385-388. [cited by applicant]
International Search Report and Written Opinion dated Sep. 21, 2023 in International Application No. PCT/KR2023/008621, 15 pages. [cited by applicant]
CN201980023392.4—Decision of Final Rejection mailed on May 17, 2024, 10 pages. [cited by applicant]
CA3,093,885—Office Action mailed on Jun. 3, 2024, 4 pages. [cited by applicant]
JP2022-211105—Decision of Rejection mailed on May 14, 2024, 3 pages. [cited by applicant]
U.S. Appl. No. 17/052,952—Non-Final Office Action mailed on Jun. 13, 2024, 20 pages. [cited by applicant]
AU2021320569—Examination Report No. 1 mailed on Apr. 30, 2024, 3 pages. [cited by applicant]
CN2021800300979—First Office Action mailed on Jan. 16, 2024, 18 pages. [cited by applicant]
MX/a/2020/009824—Office Action mailed on Jun. 10, 2024, 22 pages. [cited by applicant]
TW111145281—First Office Action mailed on May 29, 2024, 16 pages. [cited by applicant]
Bazhenova et al., Cancer Research, vol. 77, No. 13, suppl. Abstract No. CT032. [cited by applicant]
TW111128188—First Office Action mailed on May 29, 2024, 24 pages. [cited by applicant]
TW110102662—Office Action mailed on May 3, 2024, 22 pages. [cited by applicant]
TW111136059—Office Action mailed on May 3, 2024, 20 pages. [cited by applicant]
VN1-2021-06635—Office Action mailed on Feb. 26, 2024, 4 pages. [cited by applicant]
Office Action dated Jul. 9, 2021 in Taiwanese Patent Application No. 109119328. [cited by applicant]
JP2023026863—Decision of Refusal mailed on Oct. 8, 2024, 4 pages. [cited by applicant]
KR20207024813—Request for the Submission of an Opinion mailed on Jul. 30, 2024, 14 pages. [cited by applicant]
EP21853474.1—Extended European search report mailed on Jul. 31, 2024, 14 pages. [cited by applicant]
Butler M., “Optimisation of the Cellular Metabolism of Glycosylation for Recombinant Proteins Produced by Mammalian Cell Systems”, Cytotechnology, vol. 50, No. 1-3, Jun. 9, 2006, pp. 57-76. [cited by applicant]
Hossler et al., “Optimal and consistent protein glycosylation in mammalian cell culture”, Glycobiology, vol. 19, No. 9, Jun. 3, 2009, pp. 936-949. [cited by applicant]
JP2021-567961—Decision to Grant a Patent mailed on Oct. 8, 2024, 7 pages. [cited by applicant]
TW110102662—Second Office Action mailed on Sep. 5, 2024, 6 pages. [cited by applicant]
TW111136059—Second Office Action mailed on Sep. 5, 2024, 6 pages. [cited by applicant]
TW112123526—Second Office Action mailed on Sep. 6, 2024, 6 pages. [cited by applicant]
AU2023200324—Examination Report No. 1 mailed on Aug. 22, 2024, 2 pages. [cited by applicant]
EP20776465.5—Communication pursuant to 94(3) EPC mailed on Jul. 16, 2024, 7 pages. [cited by applicant]
KR20240036308—Written Decision on Registration mailed on Sep. 2, 2024, 6 pages. [cited by applicant]
BR1120200190411—Office Action mailed on Oct. 15, 2024, 8 pages. [cited by applicant]
AU2021320569—Notice of Acceptance mailed on Sep. 20, 2024, 4 pages. [cited by applicant]
CN202180030097.9—Second Office Action mailed on Oct. 13, 2024. [cited by applicant]
U.S. Appl. No. 16/628,258—Notice of Allowance mailed on Aug. 16, 2024, 8 pages. [cited by applicant]
Petition for Post Grant Review filed Nov. 12, 2024 in Case No. PGR2025-00003, U.S. Pat. No. 11,952,600. [cited by applicant]
File History of U.S. Pat. No. 11,952,600. [cited by applicant]
Declaration of Michael Hecht, Ph.D. Executed Nov. 12, 2024, Case No. PGR2025-00003, U.S. Pat. No. 11,952,600 (Exhibit 1003 in PGR2025-00003). [cited by applicant]
Declaration of Dr. Sheldon Park Executed Nov. 8, 2024, Case No. PGR2025-00003, U.S. Pat. No. 11,952,600 (Exhibit 1004 in PGR2025-00003). [cited by applicant]
Stern et al., “The Hyaluronidases: Their Genomics, Structures, and Mechanisms of Action,” Chem. Rev. 106:818-839 (2006). [cited by applicant]
Jedzrejas et al., “Structures of Vertebrate Hyaluronidases and Their Unique Enzymatic Mechanism of Hydrolysis,” Proteins: Structure, Function and Bioinformatics, 61:227-238 (2005). [cited by applicant]
Zhang et al., “Hyaluronidase Activity of Human Hyal1 Requires Active Site Acidic and Tyrosine Residues,” J. Biol. Chem., 284(14): 9433-9442 (2009). [cited by applicant]
Bordoli et al., “Protein structure homology modeling using SwissModel workspace,” Nature Protocols, 4(1):1-13 (2008). [cited by applicant]
Brandon & Tooze, “Introduction to Protein Structure,” Second Ed., Chapters 1-6, 11-12, 17-18 (1999). [cited by applicant]
Table Associating Citations from the U.S. Pat. No. 11,952,600 Patent (Exhibit 1001 in PGR2025-00003) to Corresponding Citations in U.S. Appl. No. 13/694,731 Application (Exhibit 1026 in PGR2025-00003). [cited by applicant]
Steipe, “Consensus-Based Engineering of Protein Stability: From Intrabodies to Thermostable Enzymes,” Methods in Enzymology, 388:176-186 (2004). [cited by applicant]
Green, “Computer Graphics, Homology Modeling, and Bioinformatics,” Protein Eng'g & Design, Ch. 10, 223-237 (2010). [cited by applicant]
Hardy et al., “Assessment of contraceptive vaccines based on recombinant mouse sperm protein PH20,” Reprod., 127:325-334 (2004). [cited by applicant]
Pomering et al., “Restricted Entry of IgG into Male and Female Rabbit Reproductive Ducts Following Immunization with Recombinant Rabbit PH-20,” Am. J. Reprod. Immunol., (3):174-82 (2002). [cited by applicant]
Baba et al., “Mouse Sperm Lacking Cell Surface Hyaluronidase PH-20 Can Pass through the Layer of Cumulus Cells and Fertilize the Egg,” J. Biol. Chem., 277(33):30310-4 (2002). [cited by applicant]
Primakoff et al., “Reversible Contraceptive Effect of PH-20 Immunization in Male Guinea Pigs,” Biol Reprod., 56(5):1142-6 (1997). [cited by applicant]
Tung et al., “Mechanism of Infertility in Male Guinea Pigs Immunized with Sperm PH-20,” Biol. Reprod., 56(5):1133-41 (1997). [cited by applicant]
Rosengren et al., “Recombinant Human PH20: Baseline Analysis of the Reactive Antibody Prevalence in the General Population Using Healthy Subjects,” BioDrugs, 32(1):83-89 (2018). [cited by applicant]
U.S. Appl. No. 13/694,731. [cited by applicant]
Gmachl et al., “The human sperm protein PH-20 has hyaluronidase activity,” FEBS Letters, 3:545-548 (1993). [cited by applicant]
Sills, “Retraction,” Science, 319:569 (2008). [cited by applicant]
Yue et al., “Loss of Protein Structure Stability as a Major Causative Factor in Monogenic Disease,” J. Mol. Biol., 353:459-473 (2005). [cited by applicant]
Wang & Moult “SNPs, Protein Structure, and Disease,” Hum. Mutation, 17:263-270 (2001). [cited by applicant]
“Negative Results,” Nature: Editorials, 453:258 (2008). [cited by applicant]
Lins et al., “Analysis of Accessible Surface of Residues in Proteins,” Protein Sci., 12:1406-1417 (2003). [cited by applicant]
Hayden, “Chemistry: Designer Debacle,” Nature, 453:275-278 (2008). [cited by applicant]
Benkert et al., “Toward the Estimation of the Absolute Quality of Individual Protein Structure Models,” Bioinformatics, 27:343-350 (2010). [cited by applicant]
Schwede et al., “SWISS-MODEL: An Automated Protein Homology-Modeling Server,” Nucleic Acids Rsch., 31:3381-3385 (2003). [cited by applicant]
Alberts, “Molecular Biology of the Cell,” Fifth Edition, Chapter 3 (2007). [cited by applicant]
He et al., “NMR Structures of Two Designed Proteins with High Sequence Identity but Different Fold and Function,” PNAS, 105:14412-14417 (2008). [cited by applicant]
Alexander et al., “A Minimal Sequence Code for Switching Protein Structure and Function,” PNAS, 106:21149-21154 (2009). [cited by applicant]
Ruan et al., “Design and Characterization of a Protein Fold Switching Network,” Nature Comm., 14 (2023). [cited by applicant]
Sievers et al., “Fast, Scalable Generation of High-Quality Protein Multiple Sequence Alignments Using Clustal Omega,” Molecular Sys. Biology, 7.1 (2011). [cited by applicant]
Mihel, “PSAIA—Protein Structure and Interaction Analyzer,” BMC Structural Biology, 8:21 (2008). [cited by applicant]
Redline Comparison of U.S. Appl. No. 13/694,731 application Exhibit 1026 in PGR2025-00003) and U.S. Pat. No. 11,952,600 Patent (Exhibit 1001 in PGR2025-00003) Specifications. [cited by applicant]
Beasley & Hecht, “Protein Design: The Choice of de Novo Sequences,” J. Biological Chemistry, 272:2031-2034 (1997). [cited by applicant]
Xiong et al., “Periodicity of Polar and Nonpolar Amino Acids is the Major Determinant of Secondary Structure in Self-Assembling Oligomeric Peptides,” PNAS, 92: 6349-6353 (1995). [cited by applicant]
Hayden, “Key Protein-Design Papers Challenged,” Nature, 461:859 (2009). [cited by applicant]
Kegg, Drug: Hyaluronidase (human recombinant), available at: https://www.genome.jp/entry/D06604, accessed Oct. 5, 2024. [cited by applicant]
Pace & Scholtz, “A Helix Propensity Scale Based on Experimental Studies of Peptides and Proteins,” Biophysical J. 75:422-427 (1998). [cited by applicant]
U.S. Appl. No. 61/631,313. [cited by applicant]
U.S. Appl. No. 61/796,208. [cited by applicant]
Hom_pre2011 (Exhibit 1053 in PGR2025-00003). [cited by applicant]
Hom_pre2011_header (Exhibit 1054 in PGR2025-00003). [cited by applicant]
Hom_pre2011_header_clean (Exhibit 1055 in PGR2025-00003). [cited by applicant]
Hom_pre2011.fasta (Exhibit 1056 in PGR2025-00003). [cited by applicant]
Ph20_pre2011.aln-clustal_num (Exhibit 1057 in PGR2025-00003). [cited by applicant]
Ph20_pre2011 Alignment html (Exhibit 1058 in PGR2025-00003). [cited by applicant]
Leisola & Turenen, “Protein Engineering: Opportunities and Challenges,” Appl. Microbiol. Biotechnol. 75:1225-1232 (2007). [cited by applicant]
Hecht et al., “De Novo Proteins from Designed Combinatorial Libraries,” Protein Sci., 13:1711-1723 (2004). [cited by applicant]
Rosengren et al., “Clinical Immunogenicity of rHuPH20, a Hyaluronidase Enabling Subcutaneous Drug Administration,” Aaps J., 17:1144-1156 (2015). [cited by applicant]
Collection of BLAST Webpages from the Internet Archive, navigable from: https://web.archive.org/web/20111022151531/http://www.clustal.org/omega/. [cited by applicant]
Collection of Clustal Omega Webpages from the Internet Archive, navigable from: https://web.archive.org/web/20111022151531/http://www.clustal.org/omega/, accessed Nov. 9, 2024. [cited by applicant]
Collection of Swiss-Model Webpages from the Internet Archive, navigable from: https://web.archive.org/web/20110519141121/http://swissmodel.expasy.org/?pid=smh01&uid=&token=, accessed Nov. 9, 2024. [cited by applicant]
Collection of PyMol Webpages from the Internet Archive, navigable from: https://web.archive.org/web/20110701072314/http://pymol.org/, accessed Nov. 7, 2024. [cited by applicant]
Declaration of Jeffrey P. Kushan dated Nov. 12, 2024, Case No. PGR2025-00003 U.S. Pat. No. 11,952,600 (Exhibit 1068 in PGR2025-00003). [cited by applicant]
Swiss Model Printout of PH20 Model, printed Nov. 10, 2024 (Exhibit 1069 in PGR2025-00003). [cited by applicant]
Swiss Model Printout of PH20 Model with D320K Mutation, printed Nov. 9, 2024 (Exhibit 1070 in PGR2025-00003). [cited by applicant]
Swiss Model Printout of PH20 Model with D320H Mutation, printed Nov. 9, 2024 (Exhibit 1071 in PGR2025-00003). [cited by applicant]
Swiss Model Printout of PH20 Model with D320R Mutation, printed Nov. 9, 2024 (Exhibit 1072 in PGR2025-00003). [cited by applicant]
Swiss Model Printout of PH20 Model with D320S Mutation, printed Nov. 9, 2024 (Exhibit 1073 in PGR2025-00003). [cited by applicant]
Cited By (1)
US 12,678,492